The MicroArray Quality Control (MAQC) project shows inter- and intraplatform reproducibility of gene expression measurements

Leming Shi, Leming Shi, Laura Reid, +135

Nature Biotechnology

BioinformaticsSystems BiologyGene Expression MeasurementsEngineeringMedicine +12

Preparation and hybridization analysis of DNA/RNA from E. coli on microfabricated bioelectronic chips

Jing Cheng, Edward L. Sheldon, Lei Wu, +5

Nature Biotechnology

Dna NanotechnologyE. ColiEngineeringBioelectronicsBiotechnology +9

DNA Methylation-Mediated Repression of miR-886-3p Predicts Poor Outcome of Human Small Cell Lung Cancer

Jianzhong Cao, Yongmei Song, Nan Bi, +19

Cancer Research

Loss-of-Function Mutations in the PRPS1 Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2

Xue Zhong Liu, Dongyi Han, Jianzhong Li, +19

The American Journal of Human Genetics

Developmental BiologyGenetic DisorderPrps1 Gene CauseGeneticsMolecular Genetics +3

MicroRNAs-372/373 promote the expression of hepatitis B virus through the targeting of nuclear factor I/B

Hongyan Guo, Haiying Liu, Keith Mitchelson, +16

Hepatology

Structural Insights into Molecular Function of the Metastasis-associated Phosphatase PRL-3

Guennadi Kozlov, Jing Cheng, Edmund Ziomek, +3

Journal of Biological Chemistry

A rapid method for simultaneous multi-gene mutation screening in children with nonsyndromic hearing loss

Wan Du, Jing Cheng, Hui Ding, +3

Genomics

Early DiagnosisPediatric OtolaryngologyGeneticsAudiologyHearing Screening +10

A novel <i>DFNA5 </i>mutation, IVS8+4 A&gt;G, in the splice donor site of intron 8 causes late‐onset non‐syndromic hearing loss in a Chinese family

Jing Cheng, DY Han, Pu Dai, +15

Clinical Genetics

Functional Mutation of SMAC/DIABLO, Encoding a Mitochondrial Proapoptotic Protein, Causes Human Progressive Hearing Loss DFNA64

Jing Cheng, Yuhua Zhu, Sudan He, +15

The American Journal of Human Genetics

Mitochondrial FunctionFunctional MutationGeneticsMolecular BiologyDegenerative Disease +4

Construction of a multiplex allele-specific PCR-based universal array (ASPUA) and its application to hearing loss screening

Caixia Li, Qian Pan, Yonggang Guo, +9

Human Mutation

EngineeringGeneticsMutation DetectionDisease Gene IdentificationLoss Screening +14